HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 22314288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22314347 | HCID 22314347 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22314288 | HCID 22314288 | 46% |
Reaction Steps
A solution of 3-acetyl-2-(4-chlorophenyl)indole (53.9 mg, 0.2 mmol) and phenethylbromide (30 μL, 0.22 mmol) in tetrahydrofuran is treated with NaH (60% dispersion in mineral oil, 24 mg, 0.6 mmol) at room temperature, shaken for 6 h, quenched with saturated NaHCO3 and extracted with ethyl acetate. The extracts are combined and concentrated in vacuo to afford the title product, 34 mg (46% yield), identified by NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951881B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-6a72239c8f2746638c2c60e331cf728e |
| Source note | uspto-grants-2005_10 |